Have questions? Visit https://www.reddit.com/r/SNPedia

rs4949526

From SNPedia

Orientationplus
Stabilizedplus
Make rs4949526(C;C)
Make rs4949526(C;T)
Make rs4949526(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position29959372
is asnp
is mentioned by
dbSNPrs4949526
ebirs4949526
HLIrs4949526
Exacrs4949526
Varsomers4949526
Maprs4949526
PheGenIrs4949526
hapmaprs4949526
1000 genomesrs4949526
hgdprs4949526
ensemblrs4949526
gopubmedrs4949526
geneviewrs4949526
scholarrs4949526
googlers4949526
pharmgkbrs4949526
gwascentralrs4949526
openSNPrs4949526
23andMers4949526
23andMe allrs4949526
SNP Nexus

SNPshotrs4949526
SNPdbers4949526
MSV3drs4949526
GWAS Ctlgrs4949526
GMAF0.4339
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 20889312]
Trait
Title A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder
Risk Allele T
P-val 4E-7
Odds Ratio 1.28 [NR]